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Goldenhar Syndrome: A rare case report
Goldenhar Syndrome or oculoauriculovertebral spectrum is a complex syndrome characterized by an association of maxillomandibular hypoplasia, deformity of the ear, ocular dermoid and vertebral anomalies and the most severe form of hemifacial microsomia. Here, we describe a 26-year-old male patient wi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989570/ https://www.ncbi.nlm.nih.gov/pubmed/27601832 http://dx.doi.org/10.4103/0973-029X.185907 |
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author | Bhuyan, Ruchi Pati, Abhishek Ranjan Bhuyan, Sanat Kumar Nayak, Bikash Bishwadarshee |
author_facet | Bhuyan, Ruchi Pati, Abhishek Ranjan Bhuyan, Sanat Kumar Nayak, Bikash Bishwadarshee |
author_sort | Bhuyan, Ruchi |
collection | PubMed |
description | Goldenhar Syndrome or oculoauriculovertebral spectrum is a complex syndrome characterized by an association of maxillomandibular hypoplasia, deformity of the ear, ocular dermoid and vertebral anomalies and the most severe form of hemifacial microsomia. Here, we describe a 26-year-old male patient with unilateral hemifacial microsomia, preauricular ear tags, macrosomia on the right side of the face. |
format | Online Article Text |
id | pubmed-4989570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-49895702016-09-06 Goldenhar Syndrome: A rare case report Bhuyan, Ruchi Pati, Abhishek Ranjan Bhuyan, Sanat Kumar Nayak, Bikash Bishwadarshee J Oral Maxillofac Pathol Case Report Goldenhar Syndrome or oculoauriculovertebral spectrum is a complex syndrome characterized by an association of maxillomandibular hypoplasia, deformity of the ear, ocular dermoid and vertebral anomalies and the most severe form of hemifacial microsomia. Here, we describe a 26-year-old male patient with unilateral hemifacial microsomia, preauricular ear tags, macrosomia on the right side of the face. Medknow Publications & Media Pvt Ltd 2016 /pmc/articles/PMC4989570/ /pubmed/27601832 http://dx.doi.org/10.4103/0973-029X.185907 Text en Copyright: © 2016 Journal of Oral and Maxillofacial Pathology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Bhuyan, Ruchi Pati, Abhishek Ranjan Bhuyan, Sanat Kumar Nayak, Bikash Bishwadarshee Goldenhar Syndrome: A rare case report |
title | Goldenhar Syndrome: A rare case report |
title_full | Goldenhar Syndrome: A rare case report |
title_fullStr | Goldenhar Syndrome: A rare case report |
title_full_unstemmed | Goldenhar Syndrome: A rare case report |
title_short | Goldenhar Syndrome: A rare case report |
title_sort | goldenhar syndrome: a rare case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4989570/ https://www.ncbi.nlm.nih.gov/pubmed/27601832 http://dx.doi.org/10.4103/0973-029X.185907 |
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